Long Non-Coding RNA-ATB Attenuates the Angiotensin II- Induced Injury of Vascular Endothelial Cell

被引:0
|
作者
Wang, Miao [1 ]
Gan, Shouyi [1 ]
Li, Bin [1 ]
Wang, Yajie [2 ]
机构
[1] Hubei Univ Sci & Technol, Xian Ning Cent Hosp, Dept Cardiovasc Med, Affiliated Hosp 1, Xian Ning City, Hubei, Peoples R China
[2] Hubei Univ Sci & Technol, Xian Ning Cent Hosp, Dept Geriatr, Affiliated Hosp 1, 288 Jingui Rd, Xian Ning City, Hubei, Peoples R China
来源
ANNALS OF CLINICAL AND LABORATORY SCIENCE | 2020年 / 50卷 / 03期
关键词
lncRNA-ATB; Angiotensin II; endothelial cells; cardiovascular disease; cell viability; COLORECTAL-CANCER; ACTIVATION; APOPTOSIS; PROGNOSIS;
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objective. Long noncoding RNA activated by transforming growth factor-II (lncRNA-ATB) has been reported to have critical roles in carcinogenesis and progression of several cancers. However, the expression and biological roles of lncRNA-ATB in cardiovascular disease are still unclear. This study aimed to investigate the role of lncRNA-ATB expression in endothelial cell injury. Materials. Angiotensin II (Ang II)-induced damage to endothelial cells (ECs) plays a crucial role in the research of cardiovascular disease; it is used to treat human umbilical vein endothelial cell (HUVECs) at different concentrations. qRT-PCR is used to identify the expression of lncRNA-ATB in HUVECs. CCK-8 assay and flow cytometry analysis are performed to assess cell viability and apoptosis of HUVECs. Results. Ang II treatment down-regulated the lncRNA-ATB level in HUVECs. Meanwhile, both knockdown of lncRNA-ATB and Ang II treatment impaired the viability, and increased apoptosis rate of cells. Furthermore, overexpression of lncRNA-ATB inhibited cell apoptosis and repaired cell viability in HUVECs. Conclusion. The findings indicated that lncRNA-ATB might be associated with the development of the cardiovascular disease.
引用
收藏
页码:378 / 382
页数:5
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